Evidence map›Paper›PMID 42308658›Full record

ArticleJACC. Advances2026

Clinical Spectrum and Outcomes in Hypertrophic Cardiomyopathy With Apical Aneurysms: A Large Multicenter International Cohort.

Ethan J Rowin, Deacon Z J Lee, Mark V Sherrid, Barry J Maron, Albree F Tower-Rader, Chiara Zocchi, Hisham Ahamed, Aparna Hari, Alfred J Albano, Liza Chacko and 12 more

Abstract read
In one paragraph

Article in JACC. Advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Ethan J RowinHypertrophic Cardiomyopathy Center, Lahey Hospital and Medical Center, Burlington, Massachusetts, USA. Electronic address: Ethan.Rowin@lahey.org.
Deacon Z J LeeDivision of Cardiology, Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada; University of Toronto, Toronto, Ontario, Canada.
Mark V SherridHypertrophic Cardiomyopathy Program, Leon H. Charney Division of Cardiology, NYU Langone Health, New York, New York, USA.
Barry J MaronHypertrophic Cardiomyopathy Center, Lahey Hospital and Medical Center, Burlington, Massachusetts, USA.
Albree F Tower-RaderHypertrophic Cardiomyopathy Program, Cardiology Division, Massachusetts General Hospital, Boston, Massachusetts, USA.
Chiara ZocchiCardiomyopathy Unit, Careggi University Hospital, Florence, Italy; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Hisham AhamedAmrita Hypertrophic Cardiomyopathy Center, Amrita Institute of Medical Sciences and Research, Kochi, India.
Aparna HariAmrita Hypertrophic Cardiomyopathy Center, Amrita Institute of Medical Sciences and Research, Kochi, India.
Alfred J AlbanoDivision of Cardiology, Spectrum Health, Grand Rapids, Michigan, USA.
Liza ChackoNational Heart and Lung Institute, Imperial College, London, United Kingdom.
Amanda M VarnavaNational Heart and Lung Institute, Imperial College, London, United Kingdom.
Nadia BokhariDivision of Cardiology, Tufts Medical Center, Boston, Massachusetts, USA.
Christopher MadiasDivision of Cardiology, Tufts Medical Center, Boston, Massachusetts, USA.
Richard T CarrickJohns Hopkins Hypertrophic Cardiomyopathy Center, Division of Cardiology, Baltimore, Maryland, USA.
Jose MadrazoJohns Hopkins Hypertrophic Cardiomyopathy Center, Division of Cardiology, Baltimore, Maryland, USA.
Harry RakowskiDivision of Cardiology, Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada; University of Toronto, Toronto, Ontario, Canada.
Arnon AdlerDivision of Cardiology, Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada; University of Toronto, Toronto, Ontario, Canada.
Michael A FiferHypertrophic Cardiomyopathy Program, Cardiology Division, Massachusetts General Hospital, Boston, Massachusetts, USA.
Iacopo OlivottoCardiomyopathy Unit, Careggi University Hospital, Florence, Italy; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Daniele MasseraHypertrophic Cardiomyopathy Program, Leon H. Charney Division of Cardiology, NYU Langone Health, New York, New York, USA.
Martin S MaronHypertrophic Cardiomyopathy Center, Lahey Hospital and Medical Center, Burlington, Massachusetts, USA.
Raymond H ChanDivision of Cardiology, Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada; University of Toronto, Toronto, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundApical aneurysms in hypertrophic cardiomyopathy (HCM) have been linked to sudden cardiac death (SCD) and a nidus for thromboembolism. Uncertainty remains regarding the level of risk and significance of aneurysm size.

objectivesThe objective of the study was to determine the rate of SCD events and prevalence of apical thrombus or embolic events by size (maximum transverse dimension).

methodsApical aneurysms were identified in 510 patients from 10 centers, followed a median of 4.1 years for SCD events (SCD, appropriate implantable cardioverter defibrillator therapy, and resuscitated SCD) or development of apical thrombus/thromboembolism. Relationship between size and SCD events was analyzed using multivariable Cox proportional hazard models.

resultsIn 510 HCM patients: 19% had small aneurysms (<10 mm), 39% medium (10-19 mm), 39% large (20-39 mm), and 3% very large (≥40 mm). SCD event rate was 2.1%/year, with risk increasing with increasing aneurysm size: 0.2%/year in small, 2.3%/year in medium, 3.0%/year in large and 8.2%/year in very large (P < 0.001). On multivariable analysis, greater size was associated with SCD events, independent of other risk markers or European Society of Cardiology-SCD score. Either an embolic event (3.6% of patients) or apical thrombus (10% of patients) occurred in 13% of patients and was independently associated with greater aneurysm size, 3% in small to 25% in very large aneurysms (P < 0.001).

conclusionsIn a large cohort of HCM patients with apical aneurysms, rates of SCD events were high, with continuous relationship between size and risk. Small aneurysms (<10 mm) were associated with low risk for SCD events (0.2%/year), whereas aneurysms ≥10 mm with high risk (>2%/year). Although embolic events were uncommon, increasing aneurysm size was associated with the prevalence of apical thrombi.

Indexed as

hypertrophic cardiomyopathyimplanted cardioverter defibrillatorLV apical aneurysmssudden death

Identifiers

PMID42308658
PMCPMC13311166

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.